Variant report

Variant rs1382891
Chromosome Location chr2:168055000-168055001
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:168049600-168078800 Weak transcription Right Ventricle heart
2 chr2:168051600-168056400 Enhancers Fetal Heart heart
3 chr2:168052000-168056400 Enhancers Cortex derived primary cultured neurospheres brain
4 chr2:168053200-168055200 Enhancers Primary hematopoietic stem cells short term culture blood
5 chr2:168053400-168056000 Weak transcription Fetal Intestine Small intestine
6 chr2:168053400-168056600 Weak transcription Left Ventricle heart
7 chr2:168053400-168057800 Weak transcription Gastric stomach
8 chr2:168053600-168056000 Weak transcription Psoas Muscle Psoas
9 chr2:168053600-168065800 Weak transcription HSMMtube muscle
10 chr2:168053800-168055000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr2:168053800-168057200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr2:168054200-168055200 Weak transcription Fetal Brain Female brain
13 chr2:168054200-168058400 Enhancers Skeletal Muscle Female skeletal muscle
14 chr2:168054600-168055200 Weak transcription Skeletal Muscle Male skeletal muscle
15 chr2:168054600-168055400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
16 chr2:168054600-168056400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
17 chr2:168054600-168056800 Weak transcription Primary hematopoietic stem cells blood
18 chr2:168055000-168055200 Enhancers NHLF lung
19 chr2:168055000-168055400 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --

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